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经验公式(希尔记法):
C26H40N5O10S2·Na
化学文摘社编号:
分子量:
669.74
MDL编号:
UNSPSC代码:
12352100
NACRES:
NA.21
质量水平
方案
≥95%
表单
solid
储存温度
−20°C
SMILES字符串
[Na].O=C1NC2CSC(CCCCC(=O)NCCCCCC(=O)NCCCCCC(=O)ON3C(=O)CC(C3=O)S(=O)(=O)O)C2N1
InChI
InChI=1S/C26H41N5O10S2.Na/c32-20(27-14-8-2-4-12-23(35)41-31-22(34)15-19(25(31)36)43(38,39)40)10-3-1-7-13-28-21(33)11-6-5-9-18-24-17(16-42-18)29-26(37)30-24;/h17-19,24H,1-16H2,(H,27,32)(H,28,33)(H2,29,30,37)(H,38,39,40);/t17-,18-,19?,24-;/m0./s1
InChI key
RWNPTJCDHAXLGI-BJPAGVOZSA-N
应用
Sulfo-NHS-LC-LC-biotin finds extensive applications in scientific research for the purpose of protein labeling and detection. Its utilization in protein purification allows for the isolation of biotinylated proteins from intricate mixtures. Moreover, it plays a vital role in protein-protein interaction studies, enabling investigations into the binding affinity and specificity of proteins. Additionally, it serves as a valuable tool in protein quantification, facilitating the measurement of specific protein levels within a given sample.
特点和优势
Sulfo-NHS-LC-LC-biotin is a frequently employed chemical compound in scientific investigations aimed at examining and characterizing proteins. This compound serves as a biotinylation agent, allowing for the labeling of proteins in diverse applications, including protein purification, studies on protein-protein interactions, and protein quantification. Sulfo-NHS-LC-LC-biotin works by reacting with the primary amines of proteins to form stable amide bonds. This results in the biotinylation of the protein, which allows for the detection and isolation of the protein using streptavidin or avidin conjugated to a detection system, such as a fluorescent or radioactive label.
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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Hodgkin's lymphoma patients treated with an anti-CD25 Ricin toxin A-chain (RTA)-based Immunotoxin (RFT5.dgA) develop an immune response against the toxic moiety of the immunoconjugate. The anti-RTA antibody response of 15 patients showing different clinical features and receiving different total amounts
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We have prepared several mechanism-based affinity-labeling agents for possible use in isolating N-acetylglucosaminidase, in which an N-acetylglucosamine is linked to an o-monofluoro- or difluoro-methyl phenoxy glycoside with or without a cleavable disulfide group in the tether to biotin.
Chemical probes of extended biological structures: synthesis and properties of the cleavable protein cross-linking reagent [35S]dithiobis(succinimidyl propionate).
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